Heller's Myotomy & diaphragm question
Posted , 5 users are following.
Hi group, after suffering/managing Achalasia type 1 for 14 months, I recently agreed with my Dr. to have the Heller's Myotomy with fundoplication. My concern is how will my diaphragm heal. I am a sax player in a rock band. I love it and it takes a lot of wind/breath control. Any input you could offer on heal time or experiences with breathing, playing sports, sax or anything else that takes breath control after surgery would be most appreciated.
1 like, 6 replies
AlanJM saxjean
Posted
loretta15882 saxjean
Posted
Hi Saxjean, I had the operation February, 2017. I am so thankful, because I can eat now! Just have to be conscientious about chewing food extremely well and drinking lots of water to wash it down! I waited about four years to have surgery and messed up my esophagus. It is dilated and truncated now so it's a bit more difficult to get food down! As far as breathing, I have no problems! Of course I don't do extreme exercises or play sax, but I don't believe you will have any problems!! You will be thankfull too. Just remember, that recuperation will take a while, be patient and make sure you do everything your surgeon tells you to do!! Good luck!
donna15310 saxjean
Posted
Hello. I too, have type 1, Achalasia [paralyzed esophagus]. I think you need to ask your surgeon if the diaphragm will be involved in the Heller Myotomy & Fundoplication. I had that surgery last November, and my diaphragm, as far as I know, was not involved. Having said that, I am an ordained clergyperson, and so use my voice a lot for preaching and singing/chanting. I have found at times, a little problem with 'breath, ' but I put that down to a lower level of energy now. If you have other questions, don't hesitate to ask. There is a Patient's Guide for Achalasia, that is offered online, through OPA [Osaphageal Patients Assoc.] out of the UK. 'Alan'will be able to give you the link for that [he is with OPA] and reads the posts on this Forum. I am Canadian.
Welshcake2 donna15310
Posted
donna15310 Welshcake2
Posted
Alan from OPA, can direct you to a very helpful resource, 'A Patient's Guide to Achalasia' which you can download. I found this resource to be extremely helpful..on p.12, there is information on the 3 different types of Achalasia. I have type 1, which means my esophagus is paralyzed, no movement at all. I believe the other 2 types still have some sort of movement, and those who have 2 or 3, would be better to describe their type. I have had a Heller Myotomy & Fundoplication surgery, Nov. 2016. The 'guide' explains this well, as well as other possibilities, depending upon your 'type' and situation. Botox is helpful for some people, and not for others. I guess that is just like anything else in life. This Forum is a good place to ask questions, and for support.
AlanJM saxjean
Posted
The lower oesophageal sphincter is surrounded by the muscles of the diaphragm and I believe it is these muscles that help to give the valve effect, but you would need to check this with your surgeon because my knowledge is not that detailed.